Device and method for washing, disinfecting and/or sterilizing

ABSTRACT

A device a method, and a computer program for use in a device ( 40 ) for washing, disinfecting and/or sterilizing medical, dental, laboratory and/or pharmaceutical goods. The device comprises a chamber ( 41 ) for receiving the goods, a door ( 42 ) associated with the chamber ( 41 ) and a processing circuitry for creating and storing a track record of at least one parameter of the washing, disinfecting and/or sterilizing process performed by the device ( 40 ). The user interface ( 44, 45 ) is operable by the user to cause the process circuitry to electronically sign the track record, and wherein the signing of the track record is associated with at least one condition on the device ( 40 ). The device, method and computer program facilitates an easy and secure signing of a track record directly on the device.

TECHNICAL FIELD

A device and a method for washing, disinfecting and/or sterilizingmedical, dental, laboratory and/or pharmaceutical goods. The device isadapted to permit a user to electronically sign a track record createdby the device, and optionally to store the signed track record on thedevice.

BACKGROUND OF THE INVENTION

The pharmaceutical industry, hospitals, care centers, laboratories andsimilar industries and facilities are constantly struggling againstcontaminations such as bacterial infections and viral infections.Hygiene issues are constantly on the topic and continuously evaluated.One hygiene issue of special character is the washing, disinfecting andsterilization of goods, such as sterilizing medical, dental, laboratoryand/or pharmaceutical goods. The goods may be reusable goods ordisposable goods.

Reusable goods used on such facilities can be surgical equipment such asknifes, graspers, clamps, retractors, dilators, probes, scopes, drills,and saws, laboratory equipment such as bottles, bowls, condensers,funnels, flasks, pipettes and plates, or the like. Any object which isintended to be reused and which can be contaminated with hazardous orbiological substances is the subject of harsh hygiene conditions.Whenever reusable goods have been used, such as reusable medicalequipment, the reusable goods are sent for washing, disinfecting and/orsterilization.

The process of washing, disinfecting and sterilizing goods, such asreusable medical equipment mentioned above, is a very high demandingprocess in terms of the rules and regulations, facilities used, thestaff, the process parameters, the apparatuses and even the ambientenvironment surrounding the apparatuses. All restrictions and conditionsserving the purpose to reduce, or eliminate, the risk for contaminationmakes it difficult and costly to operate washing, disinfecting and/orsterilizing processes.

For example, a pharmaceutical production site may be equipped with steamgenerators, water pretreatment apparatuses, Closure processing systems,discharge systems, component washers, glassware washers, componentsterilizer, terminal sterilization systems, isolators and sterilitytesting equipment, simply to clean and sterilize different reusablemedical equipment. The cleaning and the sterilizing apparatuses arefurther usually separated in different environmental zones, eachenvironmental zone having its own environmental conditions imposedthereon. Such environmental conditions can be demands on humidity,temperature, air pressure, ventilation systems, and access to cleanwater, or the like.

Examples of different environmental areas, or zones, in which theenvironmental conditions can vary are distribution areas, receptionareas, clean areas and sterile areas.

Each area is generally separated by a zone barrier. A zone barrier canbe a physical wall which is keeping an air pressure differential, andcan sometimes be referred to as a cross-contamination wall. Across-contamination wall can be air sealed and adapted to physicallyprevent staff members from moving between the environmental areas andair to travel there between. All precautionary measures are thus takento prevent cross contamination between the environmental areas.

Some cleaning devices, such as sterilizers for example, may be of apass-through model. A pass-through sterilizer extends across a zonebarrier and permits a staff member to load goods at one end of thesterilizer and unload sterilized goods at the other end. The sterilizerthus extends across at least one zone barrier.

The harsh hygiene conditions imposed on each environmental area, thezone barriers between the environmental areas, and the limited freedomof movement between the environmental areas for the staff members,impose high demands on the apparatuses and washing, disinfection andsterilization processes used therein.

To secure that the goods is properly treated, cleaned, disinfected orsterilized, the staff member may be required to check the track record,also referred to as batch or process record. Track records are recordedby separate computers or printers and are inspected using a graph inanalog or in digital form. The staff member usually also has to make anocular inspection of the goods to secure that the goods is in goodcondition and not for example wet or damaged. When these inspectionshave been successfully carried out, the staff member prints out a trackrecord and sign it. The track record is thereafter put in a folder andfiled. However, there is nothing that stops the staff member fromreleasing the sterilized goods earlier before these inspections havebeen carried out.

There is a possibility that due to human mistakes the goods can beunloaded and released from the sterilizer without being formallyapproved. If the sterilized goods are not inspected there is a risk thaterrors or faults in the sterilization process are not discovered.Furthermore, if a formal approval is missing, it is a clear indicationthat the inspection has not been successfully or appropriately carriedout. This could have severe consequences causing non sterile orcontaminated medical, dental, laboratory and/or pharmaceutical goods tobe released.

There is thus a need to simplify the formal approving process of a batchbefore releasing the batch from the sterilizer. There is also a need toimprove the sterilizing apparatus to prevent non sterile medical,dental, laboratory and/or pharmaceutical goods to be accidentally orincorrectly released.

SUMMARY

It is an object of the present invention to provide for a device and amethod which removes, or at least reduces the above mentioned drawbacks,or which provides a useful alternative to known prior art. The object isat least partly met by a device for washing, disinfecting and/orsterilizing medical, dental, laboratory and/or pharmaceutical goodsusing a washing, disinfecting and/or sterilizing process. The devicecomprises a chamber for receiving the medical, dental, laboratory and/orpharmaceutical goods, at least one user interface permitting a user tooperate the device and a door associated with the chamber. The devicefurther comprises a processing circuitry for creating a track record ofat least one parameter of the washing, disinfecting and/or sterilizingprocess performed by the device. The user interface is operable by theuser to cause the process circuitry to electronically sign the trackrecord, and wherein the signing of the track record is associated withat least one condition on the device.

By imposing at least one condition on the device, a procedure isestablished which enforces that the sequencing of batch approval and animposed condition, such as physical release of the medical, dental,laboratory and/or pharmaceutical goods is maintained. It is a very costeffective solution compared to using separate systems. It is a robustsystem which automatically generates an electronic track record whichcan be stored by the device, e.g. a washer, disinfector, autoclave,sterilizer, itself. It can reduce the dependence on communication withseparate systems for signature and record creation. Furthermore, itremoves the need for print outs and storage, and separate trackingsystem of paper copies.

The present invention is based on a belief that the procedure, anddevice, for quality securing that the medical, dental, laboratory and/orpharmaceutical goods has been properly washed, disinfected and/orsterilized may include the steps of; inspection, approval, releaseand/or generation of an electronically signed track record optionally incombination with an audit trail. Each of the steps can be conditioned.The condition can further be suppressed, activated, and/ or revealed, bythe electronic signing of the track record.

According to an aspect, the condition is imposed on the door of thedevice. This condition is related to the release of the medical, dental,laboratory and/or pharmaceutical goods. A condition imposed on the doorof the device can be permitting the opening and/or permitting closing ofthe door of the device. For example as the user has signed the trackrecord on the user interface, the device unlocks the door, permitting auser to open the door and unload the medical, dental, laboratory and/orpharmaceutical goods loaded in the device. A condition, in addition oroptionally, can be that the door is opened or closed by the deviceitself.

According to an aspect, a check list can be displayed on the userinterface, preferably after or before the washing, disinfecting and/orsterilizing process is initiated or completed. The check list can beinteractive so that the user can “tic” when a point on the check list isperformed or checked. When the check list is completed, e.g. the door ofthe device can be opened or permitted to be opened so that the good canbe loaded or released. The check list can be a standard check list or acustomised check list, e.g. customised by the user. The check list canbe displayed before or after the signing is performed.

According to an aspect, The device has two doors one for loading goodsfrom a non sterile or a contaminated side and one door used to unloadthe cleaned or sterilized goods. The door in the loading side cannot beopened before the door on the unloading side has been opened and closedindicating that the processed goods has been removed. If an one doorsolution is used to bout load and unload the goods it is up to the userto secure that the track record is properly signed.

According to an aspect, the at least one user interface is integratedwith the device, optionally the user interface can comprise a mobileunit, such as a touch pad, mobile smart phone or the like. The at leastone user interface can comprise a touch-sensitive display for signingthe track record. It is advantageous if the signed track record isstored locally, at least as a backup.

According to an aspect, the signing of the track record is irreversible.It is important that when a user has signed the track record, the signedtrack record cannot be manipulated or changed afterwards. At least theidentity of the signer and/or date of approval should not be able to beremoved or manipulated from the track record, so that traceability andaudit of stored track records are not only possible, but can beperformed without the risk of signed track records being accidentally orintentionally manipulated.

According to an aspect, the at least one parameter of the process istemperature, pressure, time, volume such as washing liquid volume,rinsing water volume, concentrations, pH, media quality, ions in thewashing water (hardness), consumables such as detergents, salt, or thelike. One or more parameters for creating a track record can beselected.

The track record can of course include an audit trail comprisingidentification and time and date of important events. Both the audittrail and the other selected one or more parameters are thuselectronically signed.

According to an aspect, the device is a sterilizing device. The processis in this case a sterilizing process. The device can also be a highlevel disinfection device, the process being a high level disinfection(HLD) process for the reprocessing of semi-critical devices, includingflexible endoscopes, or for sterilization of critical or semi-criticaldevices that are 30 heat-sensitive or incompatible with traditionalsterilization methods. Endoscope reprocessing, for instance, involvesthe cleaning and disinfection of endoscopes, and may encompass the stepsof cleaning, rinsing, disinfection, secondary rinsing, drying andstoring. For drying, a drying cabinet is commonly utilized, which dryingcabinet may comprise a door, a cabinet, a control circuit and a loadingsystem such as one or several shelves or hooks. Use of the dryingcabinet enables for immediate reuse of e.g. endoscopes, even afterextended storage periods thereof. Drying cabinets may comprises theinvention as described herein.

The present invention also relates to a method for electronicallysigning a track record of a process for washing, disinfecting and/orsterilizing medical, dental, laboratory and/or pharmaceutical goodsperformed by a device. The device comprises a chamber for receiving themedical, dental, laboratory and/or pharmaceutical goods, at least oneuser interface to operate the device, at least one door associated withthe chamber, and a processing circuitry for creating a track record ofat least one parameter of the process performed by the device. Themethod comprises;

-   -   registering at least one parameter of the process;    -   forming a track record based on the registration;    -   electronically signing the track record via the user interface;    -   imposing a condition on the device based on the electronically        signing of the track record.

By imposing at least one condition on the device and associate thatcondition with the signing of the track record which is equivalent witha user accepting or acknowledging that the medical, dental, laboratoryand/or pharmaceutical goods has been washed, disinfected and/orsterilized in an acceptable manner or to an acceptable level ofpureness, a procedure is established which enforces that the sequencingof batch approval and an imposed condition, such as physical release ofthe medical, dental, laboratory and/or pharmaceutical goods, ismaintained.

The method can be manipulated so that an electronic track record isautomatically generated for the user to be signed. The signed trackrecord can thereafter be stored by the device, e.g. on anautoclave/sterilizer, itself. The method reduces the dependence oncommunication with separate systems for signature and record creation.Furthermore, it removes the need for print outs and storage of papercopies.

According to an aspect, the condition is associated with the door of thedevice. The method can thus include the step of; opening the door of thedevice after the electronically signing the track record via the userinterface is performed, or permitting the door to be opened after theelectronically signing the track record via the user interface isperformed.

The method can additionally or optionally include the step of; closingthe door of the device after the electronically signing the track recordvia the user interface is performed, or permitting the door to be closedafter the electronically signing the track record via the user interfaceis performed. This step will prevent any user from starting the deviceuntil the track record has been signed, as the door to the chambercannot be closed until the signing is complete. In an embodiment, a newprocess cannot be started before the track record of the previousprocess has been formally approved, or disapproved, by signing thedisplay of the device. This is especially valuable for one door systemswhere there are limited means to ensure that the user signs the trackrecord before proceeding and release the goods.

According to an aspect, the method is disinfection or sterilizingprocess performed by the device. The device can be a dedicatedsterilizing device.

According to an aspect, the present invention relates to a computerprogram product for use in a device for washing, disinfecting and/orsterilizing medical, dental, laboratory and/or pharmaceutical goods. Thedevice comprises a chamber for receiving the medical, dental, laboratoryand/or pharmaceutical goods, at least one user interface permitting auser to operate the device, at least one door associated with thechamber, a processing circuitry for creating a track record of at leastone parameter of the washing, disinfecting and/or sterilizing processperformed by the device. The computer program product comprises codeinstructions configured for execution by the processing circuitry andwhich code instructions when executed in the device causes the device topermit a user via the user interface to electronically sign the trackrecord, and associate the signing of the track record with at least onecondition on the device.

The computer program product can be in the form of a data carriercarrying computer program code for performing the embodiments hereinwhen being loaded into the device. One such carrier may be in the formof a CD ROM disc, a memory stick, a server or other suitable carriers ormedium. The computer program code may furthermore be provided as aprogram code on a server and downloaded to the device, and executable onthe device. The device may further comprise a memory comprising one ormore memory units.

Generally, it is possible that at least one signature is required. In anembodiment two or more signatures are required to sign the track recordto impose the condition on the device. The signatures may be by the sameperson or it may be required that two unique persons sign. It is alsopossible that the condition imposed on the device is that an additionalsigning is required.

BRIEF DESCRIPTION OF THE DRAWINGS

Non-limiting embodiments of the present invention will be described ingreater detail with reference to the accompanying figures in which;

FIG. 1 shows a schematic illustration of a facility for washing,disinfecting and sterilizing medical, dental, laboratory and/orpharmaceutical goods;

FIG. 2 shows a sterilizing device;

FIG. 3 shows a process flow for a sterilizing device and the flow fortracked parameters and;

FIG. 4 shows a process flow for electronically signing of the trackrecord.

DETAILED DESCRIPTION OF PREFERRED EMBODIMENTS

FIG. 1 shows a schematic view in perspective of a facility 1 adapted forcleaning, washing, disinfecting and/or sterilizing medical equipment butthe invention is applicable to medical, dental, laboratory and/orpharmaceutical goods for, or used in, Bio-Pharmaceutical Production,Medical Device Production, Bio-Medical Research and Laboratories,Hospitals (Sterile processing departments & Wards), Outsourcedsterilization, Clinics & Practice (i.e. Dentists) and/or Elderly care.

The facility 1 has in the shown embodiment different environmental areaseach serving its own specific purpose. The facility 1 comprises a dirtyor contaminated area 10, a clean area 20, and a sterile area 30. Eacharea is separated by a zone barrier adapted to restrict access betweenthe environmental areas.

The dirty area 10 is adapted to receive goods, in this case used medicalequipment such as knifes, graspers, clamps, retractors and the like,which is in the need of cleaning, washing, disinfection and/orsterilization. The dirty area 10 is in the shown case also a receptionarea for the used medical equipment. A first zone barrier 11, in theform of a cross contamination wall, separates the dirty area 10 from theclean area 20. As can be seen, the first zone barrier 11 restricts allstaff members from direct access between the dirty area 10 and the cleanarea 20 to prevent accidental contamination between the areas.

A washer 12 to clean the used medical equipment is arranged in the zonebarrier 11. The washer 12 is of a pass through model, permitting staffmembers to load the washer 11 in the dirty area 10, and staff members tounload the washer in the clean area 20 after the used medical equipmenthas been washed. The used medical equipment is now deemed to be cleanedand thus referred to as clean medical equipment.

When a staff member unloads the washed and disinfected equipment in theclean area 30, the staff member, hereafter referred to as the user,might want to control and document that the cleaning process has beenperformed correctly. This is done visually and by studying a trackrecord of the cleaning process. The track record can compriseinformation such as time, and temperature curves water consumption orsimilar, so that the user can confirm that the cleaning process has beenperformed correctly. When reprocessing medical devices that cannot besterilized due to material composition, material incompatibility withthe sterilization process or heat sensitiveness it is advantageous ifthe compliance with the reprocessing method is ensured. The user canelectronically sign the track record directly on the washer 12 so thatthe medical equipment can be unloaded and released to the next station.The electronic signing, the device and method used, will be described ingreater detail below.

In the clean area 20, the clean medical equipment is arranged andprepared for further treatment. The clean medical equipment can besorted and packed in air tight bags for example. A second zone barrier21 separates the clean area 20 from the sterile area 30.

Pass through models of autoclaves 21, in this case steam sterilizers,are arranged to extend across the second zone barrier 21 for furthertreatment of the clean medical equipment. Examples of further treatmentof the clean medical equipment can be kill (effluent) cycles forpathogenic waste decontamination, well-balanced processes for openliquids to minimize loss of the product liquid, adaptation to requiredBSL level or other specific applications. In general the treatment isperformed at high temperatures using steam (but not all).

After the clean medical equipment has been sterilized it can be referredto as sterile medical equipment. The sterile medical equipment can nowbe released and is ready to be transported to a storage room at thefacility and is ready to be used again.

When a staff member unloads the sterile medical equipment in thesterilized area 30, the staff member, hereafter referred to as the user,will need to control and document that the sterilization process hasbeen performed correctly. This is done visually and by studying a trackrecord of the sterilization process. The track record can compriseinformation such as time, temperature and pressure curves or similar, sothat the user can confirm that the sterilizing process has beenperformed correctly.

FIG. 2 shows a steam sterilizer 40, hereafter referred to as thesterilizer 40, in greater detail. The sterilizer 40 can be of a one doortype or of a pass through model, having doors on opposite sides of thesterilizer permitting the sterilizer 40 to bridge across a zone barrier,such as a cross contamination wall 11, 21. The sterilizer comprises achamber 41 for receiving the medical equipment for sterilization. Aslideable door 42 is adapted to seal the chamber 41. A tray 43 isconfigured to receive the medical goods inside of the chamber. The trayis removable from the chamber 41. A user interface 44 is adapted so thatthe user can operate the sterilizer 40, in the shown embodiment a touchsensitive display is used as a user interface.

Sterilization (or sterilisation) herein relates to a process thateliminates, removes or kills microbial life, including transmissibleagents (such as fungi, bacteria, viruses, spore forms, etc.) present ona surface, contained in a fluid, in medication, and/or on and/or in acompound such as biological culture media. Sterilization can be achievedby applying heat, chemicals, irradiation, high pressure, and filtrationor combinations thereof.

Steam sterilization, or autoclaving, involves subjecting goods to steamat a high temperature. Steam sterilization involves the use of saturatedsteam under pressure and is a non-toxic method for sterilization.Further, steam sterilizers (autoclaves) are available in different sizesfor different purposes.

Four factors are relevant for the outcome of steam sterilization: steam,pressure, temperature and time. The device 40 for washing, disinfectingand/or sterilizing medical, dental, laboratory and/or pharmaceuticalgoods using a washing, disinfecting and/or sterilizing process, shouldpreferably be adapted to operate at a temperature above 100° C.,preferably above 120° C., more preferably between 120-140° C. and atsuitable pressure, at least above 101,3 kPa, or corresponding pressurefor saturated steam. A sterilizer disclosed herein should preferably atleast meet the requirement of EN285:2006 and A2:2009, standards used inthis field of technology and known to the skilled person in the art.

The sterilisation time required varies depending on the goods to besterilised, sterilisation time necessary at a defined temperature willalso depend on the goods to be sterilised. Chemical and biologicalindicators are available for monitoring the sterilisation process and toensure that sterility is achieved. Properly executed steam sterilisationwill inactivate all fungi, bacteria, viruses and bacterial spores. Ifnot all fungi, bacteria, viruses and bacterial spores can beinactivated, the temperature, time and pressure is selected so that thesterilization device, and the method, has a Sterility assurance level,SAL, of at most 1/1.000.000, preferably lower than 1/1.000.000. SAL isused to describe the probability of a non sterile unit exiting thedevice or method after the sterilization process has been completed.

The sterilizer 40 comprises a process circuitry (not shown) for creatinga digital track record of the sterilizing process. The track record ismade by registering at least one parameter of the sterilizing processsuch as temperature, pressure, time, volume such as washing liquidvolume, rinsing water volume, or the like. The registering can be doneby means of recording measurements of the at least one parameter, whichare stored locally or remotely. If stored remotely, the sterilizers 40comprises a communication unit adapted to forward the track record, orparts thereof, to the remote storage device. By locally is meant thatthe rack record is stored in the sterilizing device itself on a storagedevice such as hard drive or similar.

A sterilizing process is generally including but not limited to thesteps of; loading the medical, dental, laboratory and/or pharmaceuticalgoods to be sterilized, choosing a sterilizing program, performing thesterilizing process, unloading the sterilized medical, dental,laboratory and/or pharmaceutical goods. Somewhere after the sterilizingprocess is completed, or partly completed, the user may want to inspectthat the sterilizing process has been performed correctly. Theinspection can be made by visually viewing a temperature/time graphtracking the steam temperature during the sterilization process, or byviewing a computer generated parameter(s), value(s) or graph(s),associated with the registered track record. In case of a graph, thegraph can be plotted directly on the user interface, in this case thetouch sensitive display 44. The user can thereafter acknowledge that thetrack record has been controlled and accepted. The acknowledgement isperformed by electronically signing the track record, e.g. digitallysigning the track record.

The electronically signing of the track record can be done using apersonal and/or group identification sign. Examples of a personalidentification sign are identification signs which are unique for oneindividual while a group identification sign can be used by a limitednumber of people e.g. 2-20 users. In the latter case the group of peopleis generally authorized to sign the track record. Examples ofidentification signs are personal codes such as identification numbers,names, passwords or similar, finger prints, voice recognition, eyereticule identification, or the like.

FIG. 3 shows a schematic diagram of a sterilizing process comprising thethree distinct states, FIG. 3 shows; a stand by state 100, an in processstate 110 and; a process complete state 120. Please notice that thesterilization process can comprise additional steps other than thosedescribed herein.

With reference to FIGS. 2 and 3; with the stand by state 100, the useris free to load a batch of the sterilizing device 40 with the medical,dental, laboratory and/or pharmaceutical goods to be sterilized. Anappropriate sterilization program is selected on the program selectionmenu displayed on the user interface 44, in this case a touch screen 45.When the appropriate program is selected, the graphical interactiveuser-interface object representing a start button is activated on thetouch screen so that the user can start the sterilization program. Hencea graphical interactive user-interface object which is relevant for thecurrent state of the sterilizing process is displayed, while at leastone graphical interactive user-interface object not relevant for thecurrent state is inactivated. A user is now free to start thesterilization program. As an alternative, the program to select andstart can be controlled by a separate device such as an automaticloading system or similar.

After the sterilization program has been initiated, the sterilizationdevice 40 is in process state 110. In this state the sterilizationdevice 40 initiates and performs the sterilization program to sterilizethe medical, dental, laboratory and/or pharmaceutical goods in thechamber 41. In this state, the user interface displays the remainingtime of the sterilization program and the only graphical interactiveuser-interface object which is activated for use is a cancel function.Exceptions may be for graphical interactive user-interface objects whichare not related to the sterilizing process, such as general menubuttons.

When the sterilizing device 40 has finished the sterilization program,the sterilization device 40 enters the process complete state 120. Inthe process complete state, the user may open the door 42 to access thechamber 41 of the sterilizing device 40.

The process circuitry is adapted to register different parameters duringthe sterilization process. For example, during the standby state 100,the process circuitry can register stand by related parameters 200 suchas the weight or position of the medical, dental, laboratory and/orpharmaceutical goods loaded in the chamber 41 of the sterilizationdevice 40, the current temperature or status of a heating element forthe steam generator, the time elapsed since the last sterilizationprogram was performed, or similar.

During the in process state 110, the process circuitry can registersterilization program related parameters 210 such as temperature,pressure, time, incoming media quality, or the like. The registration isperformed using at least one sensor. The sensors and how to registereach parameter are known per se and will not be discussed furtherherein.

Examples of other parameters are volume such as washing liquid volume,rinsing water volume, consumables such as detergents, pH, saltconcentration.

In the process complete state 120, the process circuitry can registerpost sterilization program related parameters such as if the door isopened or closed, medical, dental, laboratory and/or pharmaceuticalgoods is unloaded, measuring time from when the program is finished orthe like.

When the track record is created or subsequently after, the user isinvited to electronically sign the track record 300.

FIG. 4 shows a non-limiting embodiment of how the box 300 (FIG. 3) canbe configured. As mentioned, the sterilizing device 40 is adapted topermit a user to electronically sign the track record using the userinterface of the sterilizing device 40.

A language conversion circuitry 301 converts the registered data into anacceptance format data for picture conversion. A picture generatingcircuitry 302 is used to convert the acceptance format data into apicture. The picture is displayed on a user interface display unit 303.The user interface display unit 303 is the user interface 44, in thiscase the touch screen 45 shown in FIG. 2. The user can sign his or hersname directly on the user interface display unit 303. Optionally theuser interface display unit 303 displays a graphical interactiveuser-interface object or, such as an alphanumeric pad or similar,permitting the user to enter credentials as for example a code and anuser ID to confirm who approved that the sterilization program has beenperformed in an acceptable manner. If an alphanumeric pad is used, theuser could enter one or several codes representative for the identity ofthe user and an approval of the process.

A signature identification circuitry 304 identifies the signature andthus the identity of the user who signs the user interface display unit303. The identification can be made by comparison with locally storeddata or with remotely stored data.

The PDF conversion circuitry 305 converts the signed acceptance formatdata into a PDF file or other similar tamper proof format. A tamperproof electronically signed file of the track record is now formed. Thetamper proof electronically signed file of the track record can bestored locally on a hard drive or remotely in a cloud or on a server.The tamper proof electronically signed file of the track record can bestored together with additional information such as the date and time,identification information of the medical, dental, laboratory and/orpharmaceutical goods which has been sterilized, batch number, andoptionally at least one more parameter such as the selectedsterilization program, or the like. Optionally such additionalinformation is included in the track record and is thus signed togetherwith the track record.

Optionally the user can use voice recognition for signing the trackrecord, other methods of electronically signing is also possible.

The signing of the track record triggers at least one condition 307. Thecondition can be triggered when the signature identification circuitry304 has identified the identity of the user, when the PDF conversion iscomplete, or when the signed track record is archived, i.e. stored, forexample.

With reference to FIG. 2, the at least one condition can be that theuser is enabled to open or close the door 42 to the chamber 41, or itcan be that the sterilization device 40 open or close the door 42 to thechamber 41. In a preferred embodiment, the condition is associated withthe door 42 of the chamber 41 of the sterilization device, preventing auser to open or close the door 42 to the chamber 41. It could optionallyor additionally be that the user interface display unit is preventedfrom other input data until the signing is complete.

The imposed condition with the signing of the track record will preventa batch of medical, dental, laboratory and/or pharmaceutical goods frombeing released without a user controlling that the sterilization programhas been performed in a predetermined manner, or in an acceptablemanner. In an embodiment, this is done by preventing the door 42 frombeing opened before the track record of the sterilization process issigned by the user. In another embodiment the sterilization device 40 isprevented from being loaded with new medical, dental, laboratory and/orpharmaceutical goods to be sterilized before the track record of thesterilization process has been signed by preventing the door 42 frombeing closed. If a two door system is used the unloading door could beprevented from being closed until the track record is signed. With theunloading door being open the loading door cannot be opened prohibitingnew goods being loaded in to the machine and a new process started.

After the signature has been done, the signed document cannot bemanipulated in the sense that the signing of the track record isirreversible, preferably for everybody, but at least for the useridentified through the signature.

Other conditions are possible in combination or alone, to prevent thegoods, in this case the medical equipment, from being unloaded from thedevice, or released from the specific area, to ensure thatinsufficiently washed, disinfected or sterilized goods, or contaminatedgoods, accidentally leaves the sterile area 30.

Optionally, or additionally, the device is tamper proof in terms of thatonly authorized staff has access to, and is permitted to use, thedevice. Optionally or additionally, all regulated data is maintained,can be reconstructed and can be readily retrieved. Optionally oradditionally, the uniqueness of authentications (e.g., User ID andPassword combinations) regarding using the device and applyingelectronic signatures can be guaranteed.

Optionally or additionally, electronic signatures cannot be removed,copied/pasted to other electronic records or otherwise tampered with.

1. A device for washing, disinfecting and/or sterilizing medical,dental, laboratory and/or pharmaceutical goods using a washing,disinfecting and/or sterilizing process, said device comprising achamber for receiving said medical, dental, laboratory and/orpharmaceutical goods, at least one user interface permitting a user tooperate said device, a door associated with said chamber, processingcircuitry for creating a track record of at least one parameter of saidwashing, disinfecting and/or sterilizing process performed by saiddevice, wherein said user interface is operable by said user to causesaid process circuitry to electronically sign said track record by usinga personal and/or group identification sign, and wherein said signing ofsaid track record is associated with at least one condition on saiddevice.
 2. The device according to claim 1, wherein said condition isimposed on said door.
 3. The device according to claim 2, wherein saidcondition is permitting opening and/or permitting closing of said doorof said device.
 4. The device according to claim 1, wherein saidcondition is opening or closing said door of said device.
 5. The deviceaccording to claim 1, wherein said at least one user interface isintegrated with said device.
 6. The device according to claim 14,wherein said at least one user interface is comprised in a mobile unit.7. The device according to claim 1, wherein said at least one userinterface comprises a touch-sensitive display for signing said trackrecord.
 8. The device according to claim 1, wherein said signing of saidtrack record is irreversible.
 9. The device according to claim 1,wherein said at least one parameter of said process is selected from thelist of: temperature, pressure, time, volume such as washing liquidvolume, rinsing water volume, consumables such as detergents, pH, saltconcentration, and media quality.
 10. The device according to claim 1,wherein said condition is associated with inspection, approval, releaseand/or the generation of the electronically signed track record.
 11. Thedevice according to claim 1, wherein said device is a reprocessing,drying, washer, disinfector or sterilizing device.
 12. A method forelectronically signing a track record of a process for washing,disinfecting and/or sterilizing medical, dental, laboratory and/orpharmaceutical goods performed by a device, said device comprising achamber for receiving said medical, dental, laboratory and/orpharmaceutical goods, at least one user interface to operate saiddevice, a door associated with said chamber, processing circuitry forcreating a track record of at least one parameter of said processperformed by said device, said method comprising: registering at leastone parameter of said process; forming a track record based on saidregistration; electronically signing said track record via said userinterface by using a personal and/or group identification sign; imposinga condition on said device based on said electronically signing of saidtrack record.
 13. The method according to claim 12, wherein saidcondition is associated with said door of said device.
 14. The methodaccording to claim 13, wherein said method further comprises permittingsaid door to be opened and/or closed.
 15. The method according to claim12, wherein said method is a drying, washing, disinfection orsterilizing process performed by said device.
 16. A computer programproduct for use in a device for drying, washing, disinfecting and/orsterilizing medical, dental, laboratory and/or pharmaceutical goods,said device comprising a chamber for receiving said medical, dental,laboratory and/or pharmaceutical goods, at least one user interfacepermitting a user to operate said device, a door associated with saidchamber, a-processing circuitry for creating a track record of at leastone parameter of said drying, washing, disinfecting and/or sterilizingprocess performed by said device, wherein said computer program productcomprises code instructions configured for execution by said processingcircuitry and which code instructions when executed in said devicecauses said device to permit a user via said user interface toelectronically sign said track record by using a personal and/or groupidentification sign, and associate said signing of said track recordwith at least one condition on said device.